Senior Manager, Quality Engineering

Abbott

Minnetonka, Minnesota, United States
Base: $129,300.00 – $258,700.00; bonus/equity: not...
Not specified (assumed hybrid based on company culture and role)
Minimum 10 years related work experience
Minimum 5 years people management experience
Experience with gmps glps and gcps
Abbott is seeking a Senior Manager for Quality Engineering in Minnetonka, Minnesota, to lead the quality engineering department within their Electrophysiology business. The ideal candidate will have significant experience in regulatory requirements and people management, contributing to the development of quality systems that meet internal and external standards

Job Summary

  • This role provides leadership for the quality engineering department supporting commercial products and new product development in the Electrophysiology business.
  • The position is responsible for developing goals, objectives, procedures, policies, and systems that align with FDA/ISO regulations and company mission.
  • Employees qualify for free medical coverage in the Health Investment Plan, an excellent retirement savings plan, and tuition reimbursement benefits.

Matching Summary

Match Score: 85

Abbott is seeking a Senior Manager for Quality Engineering in Minnetonka, Minnesota, to lead the quality engineering department within their Electrophysiology business. The ideal candidate will have significant experience in regulatory requirements and people management, contributing to the development of quality systems that meet internal and external standards.

Salary

Base: $129,300.00 – $258,700.00; Bonus/Equity: Not specified; Benefits: Free medical coverage, retirement savings plan, tuition reimbursement

Skills & Requirements

Must-have

  • Minimum 10 years related work experience
  • Minimum 5 years people management experience
  • Experience with GMPs GLPs and GCPs
  • Domestic and International regulatory requirements
  • FDA and ISO regulations compliance

Nice-to-have

  • Prior experience in medical device manufacturing
  • MBA preferred qualification
  • Familiarity with TUV regulations
  • Class III or II medical device background
  • ISO 9001 and ISO 13485 knowledge

Key Requirements

  • Bachelors Degree in related field
  • Minimum 10 years related work experience
  • Minimum 5 years people management experience
  • Experience working in regulated environment
  • Ability to travel internationally 10%

Work Rights

Not specified

Tailored Resume

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